A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571061



Internal ID20944132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10830565..10831283hg38UCSC Ensembl
chr5:10830677..10831395hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571061
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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